Background-Transcatheter pulmonary valve (TPV) replacement is an emerging therapy intended to restore pulmonary valve function in patients with right ventricular outflow tract conduit dysfunction; the impact of this technique on ventricular strain and synchrony is not known. Methods and Results-Cardiac magnetic resonance and ECG data acquired at 1 center as part of the US Melody TPV trial were analyzed. Biventricular strain and mechanical synchrony measurements were made based on short-axis and 4-chamber steady-state free precession images using feature tracking software. Post-versus pre-TPV replacement findings were compared for all patients (n=31) and subgroups with predominant pulmonary regurgitation (n=13) or stenosis (n=18). Most patients had tetralogy of Fallot (18/31). After TPV replacement, left ventricular (LV) circumferential strain increased for the whole cohort (P<0.001) and both subgroups (pulmonary regurgitation P=0.01; pulmonary stenosis P=0.02). LV longitudinal strain increased for the whole cohort (P=0.02) and pulmonary regurgitation subgroup (P=0.05); circumferential right ventricular strain increased for the pulmonary stenosis group only (P=0.05). LV longitudinal synchrony improved significantly in the pulmonary regurgitation group (maximum wall delay P=0.03; cross-correlation delay P=0.01). Electric measures of synchrony did not improve.
Conclusions-In
Harrild et al
Impact of TPV Replacement 681are no reports of any kind of its impact on synchrony of the left ventricle (LV) or RV. The goal of the present study was to quantify the impact of TPV replacement on indices of RV and LV strain and synchrony in patients with dysfunctional RVOT conduits using high-quality CMR images.
Methods
Study DesignThis was a retrospective cohort study of patients undergoing placement of a Melody TPV in the setting of a dysfunctional RVOT conduit designed to investigate changes in ventricular mechanics based on CMR images before and after pulmonary valve implantation. This study was performed according to a protocol approved by the Committee for Clinical Investigations at Boston Children's Hospital, Boston, MA.
PatientsPatients included in this study comprised a subset of the cohort enrolled at our center as part of the multicenter US Melody TPV investigational device exemption (IDE) trial. Briefly, the IDE trial was designed to investigate the safety, procedural success, and short-term effectiveness of Melody valve placement in patients with a biventricular circulation and a dysfunctional RVOT conduit. Study protocols and short-term outcomes have been previously reported. 4,5 As part of their participation in the trial, patients had clinical, ECG, and CMR data collected before and 6±2 months after TPV replacement. Patients were included in the present study if they had high-quality CMR images for analysis both pre-and post-TPV replacement performed between 2007 and 2010.Patients were first analyzed as an entire cohort, and then dichotomized into 2 groups: predominant pulmonary stenosis (PS; RVOT peak systolic e...